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FDA 510(k)

FLOWTRON AC200/2

K-Number: K874688 · 1988-09-23

ApplicantHuntleigh Technology, Inc.
Decision Date1988-09-23
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FLOWTRON AC200/2 is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Technology, Inc.. It received FDA 510(k) clearance on 1988-09-23 under 510(k) number K874688. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOWTRON AC200/2?

FLOWTRON AC200/2 is a medical device that received FDA 510(k) clearance on 1988-09-23. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K874688.

When did FLOWTRON AC200/2 receive FDA 510(k) clearance?

FLOWTRON AC200/2 received FDA 510(k) clearance on 1988-09-23, under 510(k) number K874688.

Who is the listed applicant for FLOWTRON AC200/2?

The FDA 510(k) record lists Huntleigh Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOWTRON AC200/2?

The FDA product code for FLOWTRON AC200/2 is IRP.

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Other records listing Huntleigh Technology, Inc. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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